ClinVar Miner

List of variants in gene MYH14 reported as benign for not specified

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Gene type:
ClinVar version:
Total variants: 61
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HGVS dbSNP gnomAD frequency
NM_001145809.2(MYH14):c.3033+11T>C rs930086 0.86981
NM_001145809.2(MYH14):c.5678+12C>T rs3826772 0.78229
NM_001145809.2(MYH14):c.2250A>G (p.Pro750=) rs1651553 0.74436
NM_001145809.2(MYH14):c.5469+16C>T rs3745510 0.64922
NM_001145809.2(MYH14):c.5430G>A (p.Ser1810=) rs3745509 0.63924
NM_001145809.2(MYH14):c.657G>A (p.Ala219=) rs4801822 0.56915
NM_001145809.2(MYH14):c.3018G>A (p.Leu1006=) rs3745504 0.53291
NM_001145809.2(MYH14):c.2355-14C>T rs12981413 0.46235
NM_001145809.2(MYH14):c.2205C>G (p.Arg735=) rs378811 0.38312
NM_001145809.2(MYH14):c.1114+13C>T rs11666328 0.32285
NM_001145809.2(MYH14):c.2355-17C>T rs28482851 0.23202
NM_001145809.2(MYH14):c.3680+9C>T rs76579307 0.20534
NM_001145809.2(MYH14):c.91C>A (p.Pro31Thr) rs590722 0.14959
NM_001145809.2(MYH14):c.2827-9A>C rs3745503 0.14515
NM_001145809.2(MYH14):c.4752+16G>A rs10406788 0.14474
NM_001145809.2(MYH14):c.1483-10G>A rs73061136 0.09105
NM_001145809.2(MYH14):c.1755C>T (p.Gly585=) rs61731838 0.07411
NM_001145809.2(MYH14):c.1149T>C (p.Phe383=) rs61734424 0.06194
NM_001145809.2(MYH14):c.1890C>T (p.Val630=) rs77895476 0.03277
NM_001145809.2(MYH14):c.474T>C (p.Ile158=) rs34796700 0.02809
NM_001145809.2(MYH14):c.5281C>A (p.Arg1761=) rs116035034 0.02785
NM_001145809.2(MYH14):c.2041G>C (p.Gly681Arg) rs75915336 0.02765
NM_001145809.2(MYH14):c.4753-9C>T rs45591233 0.02396
NM_001145809.2(MYH14):c.3749C>A (p.Ala1250Glu) rs11669191 0.01884
NM_001145809.2(MYH14):c.3468-3C>T rs78192108 0.01724
NM_001145809.2(MYH14):c.1024C>G (p.Pro342Ala) rs34498817 0.01645
NM_001145809.2(MYH14):c.483G>A (p.Met161Ile) rs34773557 0.01615
NM_001145809.2(MYH14):c.4596C>T (p.Ala1532=) rs35453633 0.01258
NM_001145809.2(MYH14):c.6012A>T (p.Leu2004=) rs73932457 0.01253
NM_001145809.2(MYH14):c.4741G>A (p.Val1581Ile) rs680446 0.01091
NM_001145809.2(MYH14):c.2841C>T (p.Arg947=) rs138987081 0.01050
NM_001145809.2(MYH14):c.5466G>A (p.Leu1822=) rs10419343 0.01020
NM_001145809.2(MYH14):c.5334T>C (p.Gly1778=) rs115844649 0.00878
NM_001145809.2(MYH14):c.3663C>T (p.Asn1221=) rs78573213 0.00779
NM_001145809.2(MYH14):c.5868C>T (p.Ala1956=) rs190695624 0.00710
NM_001145809.2(MYH14):c.4255C>T (p.Arg1419Trp) rs115019972 0.00553
NM_001145809.2(MYH14):c.2792G>A (p.Arg931His) rs200351672 0.00460
NM_001145809.2(MYH14):c.826A>G (p.Ile276Val) rs55645295 0.00445
NM_001145809.2(MYH14):c.2763A>G (p.Lys921=) rs191788683 0.00404
NM_001145809.2(MYH14):c.4586G>A (p.Arg1529His) rs185232438 0.00309
NM_001145809.2(MYH14):c.1150G>T (p.Gly384Cys) rs119103280 0.00303
NM_001145809.2(MYH14):c.1034C>G (p.Ser345Cys) rs35315400 0.00249
NM_001145809.2(MYH14):c.5529C>T (p.Ser1843=) rs12610591 0.00248
NM_001145809.2(MYH14):c.1329+15C>T rs200176028 0.00227
NM_001145809.2(MYH14):c.5533C>T (p.Arg1845Trp) rs199600574 0.00223
NM_001145809.2(MYH14):c.5227C>T (p.Leu1743=) rs147447646 0.00218
NM_001145809.2(MYH14):c.3079C>T (p.Leu1027=) rs113152264 0.00210
NM_001145809.2(MYH14):c.4685G>A (p.Arg1562Gln) rs140118363 0.00158
NM_001145809.2(MYH14):c.5573G>A (p.Arg1858His) rs11882073 0.00137
NM_001145809.2(MYH14):c.4094G>A (p.Ser1365Asn) rs202225655 0.00134
NM_001145809.2(MYH14):c.2432C>T (p.Ala811Val) rs201337011 0.00093
NM_001145809.2(MYH14):c.1992G>A (p.Pro664=) rs192745436 0.00086
NM_001145809.2(MYH14):c.5991G>A (p.Thr1997=) rs181567755 0.00084
NM_001145809.2(MYH14):c.5683C>T (p.Arg1895Cys) rs200485394 0.00062
NM_001145809.2(MYH14):c.4753-5A>G rs118097099 0.00036
NM_001145809.2(MYH14):c.2600G>A (p.Arg867His) rs547836952 0.00008
NM_001145809.2(MYH14):c.1205A>G (p.Asn402Ser) rs537153044 0.00001
NM_001145809.2(MYH14):c.192G>T (p.Gly64=) rs181055215
NM_001145809.2(MYH14):c.33G>C (p.Arg11=) rs8106196
NM_001145809.2(MYH14):c.5083G>C (p.Gly1695Arg) rs199915414
NM_001145809.2(MYH14):c.660G>T (p.Ser220=) rs201835322

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